Your tasks:

• You support the organization and implementation of GMP-relevant tasks within your area of ​​responsibility.
• You maintain and further develop the pharmaceutical quality assurance system within the framework of applicable GMP requirements.
• You process and track deviations, CAPA measures, and change requests in the change control system.
• You review and approve quality-relevant documents, specifications, and manufacturing and testing instructions.
• You will support qualification and validation activities in the laboratory and production areas.
• You plan, conduct, and follow up on self-inspections as well as customer and supplier audits.
• You qualify and monitor suppliers, service providers and external testing laboratories with GMP relevance.
• You organize GMP training courses and monitor their completion.
• You process and investigate quality-related complaints.
• You will support product quality reviews and GMP-relevant communication with internal and external contacts.
•